Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.
Your Role:
Design, Build, Configure and support Veeva Vault based applications to meet business process and application requirements.
Prepares communications and makes presentations on system enhancements and/or alternatives. Evaluates, optimizes, harmonizes, and standardizes existing systems.
Create and update system documentation. Monitors quality standards and ensures failure-free operation. Considers compatibility of different systems.
Solves a range of straightforward problems through knowledge and technical experience in own discipline with a moderate level of guidance.
Analyzes information and possible solutions and makes independent judgments, decisions, and recommendations.
Support the on-going regulatory compliance of the IT components for defined services.
Review and approve regulatory system changes and documentation.
Support periodic reviews of the entire system and compile related reports during operation phase.
Support the on-going regulatory compliance of the IT components for defined services
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Support the qualification activity and documentation related to IT solutions delivery
Understands how the team integrates with other teams to achieve overall objectives of the area and builds knowledge of the organization, processes, customers, and key business drivers.
Who you are:
Minimum of 6-10 years of IT experience.
Minimum of bachelor’s Degree or applicable experience within information/Computer systems.
Must have Veeva Vault skillset and having Veeva Vault RIM experience will be preferred.
Deep knowledge of Veeva Vault configuration, developing them in live projects based on client requirement.
Working knowledge of Document and Object record migration from legacy application to Veeva Vault.
Good technical knowledge in core technologies and platforms such as Java, .Net, XML, HTML, PL/SQL & API.
Previous experience in the biotechnology / Pharmaceutical / Life Science or related industry implementing and validating computer systems that manage regulated information
Working knowledge of IT infrastructure qualification processes and IT operating procedures
Solid understanding & experience in GxP, GAMP and delivering validated applications (21 CFR Part 11)
Thoroughly familiar with Quality & GxP IT compliance requirements.
Strong planning and analytical skills combined with ability to work with geographically distributed teams in a rapid development model.
Awareness of ITIL and Support Project Methodology.
Ability to familiarize himself / herself independently with entirely new subjects and thus provide comprehensive and innovative solutions
Excellent written and verbal communications skills
Working knowledge of Information security and best practices
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
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